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Paper is the most important writing carrier and its degradation (acidification, aging, and ink removal) is a major issue in the protection of cultural heritage. In this work, we first propose alkali ion-exchanged Y zeolites (Ae-Y) as superior deacidification agents for paper. Their features such as the high surface area, adjustable alkali ion content, strength, good structural stability, and safety/non-toxicity or biocompatibility are very promising for preserving paper-based materials, as demonstrated by aging experiments carried out on both historical wood-pulp paper and modern hand-made bamboo paper samples. Through H 2 O-mediated dispersion of Ae-Y in target paper samples, the pH of the paper can be modified to a neutral or weakly basic state, and can be maintained for a long time even under harsh accelerated aging conditions. Meanwhile, the Ae-Y coating hardly alters the chromatic aberration and water wettability of papers. This new deacidifying agent does not trigger color changes in alkali-sensitive pigments (i.e., does not cause fading or blanching of pigments). Moreover, a systematic evaluation of the structure-performance relationship indicates the important roles of adequate accessible basic sites and controllable and mild basicity of Ae-Y in the long-term deacidification, anti-aging, and anti-fading effects exerted on paper relics. These findings not only shed light on the design of protective materials for paper-based cultural relics but also expand our knowledge on the deacidification and protection mechanisms of zeolites. Image 1 • Alkali ion-exchanged Y zeolites are proposed as deacidifying agents for paper. • They may be better alternatives in aqueous phase than generally used MgO and CaO. • Their superior performance is due to adequate accessible and mild basic sites. • The zeolite coatings hardly alter chromatic aberration and wettability of paper. • The zeolite coatings do not cause fading or blanching of alkali-sensitive pigments. [ABSTRACT FROM AUTHOR]

[Display omitted] It is a Holy Grail to realize the goal-oriented synthesis of zeotype crystals via direct thermodynamic/kinetic control of crystallization in the simplest inorganic system. Especially, the most commonly used counter cations (i.e., Na+ and K+) are in turn believed to play merely the role of balancing charges and stabilizing frameworks, which make the simple ion-based morphology/porosity control remain big challenges. We re-examined the role of Na+ and K+ to fine-tune the classical/nonclassical crystallization process in a seed-induced system with the simplest composition (Si/Al sources, inorganic alkali, and H 2 O), and proposed an "ion switch" strategy. By analyzing the multiple growth curves, tracking the precursor evolution, and observing epitaxial crystallization behavior, a distinctive "ion switch"-worked nonclassical mechanism was uncovered. By the "ion switch" strategy, ZSM-5 mesocrystals were fine-regulated with diverse architecture from single crystal to nanocrystallite assembly and intracrystal mesopore-enriched crystal. Such simple ions-controlled crystallization was achieved through microstructure heterogeneity of zeolitic building-blocks triggered by different counterions and their corresponding assembly behavior from oriented attachment to random deposition. Furthermore, this protocol can be extended to a wider H 2 O/SiO 2 range, mixed Na+/K+ systems, and other alkali metal ions from Li+ to Cs+, and ZSM-5 mesocrystals with extended morphologies can be obtained. [ABSTRACT FROM AUTHOR]